All diseases

OMIM ID
251880
OMIM term:
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE); MTDPS3
Alternative terms:

(∗) Location:
2p13.1  
(†) Associated OMIM genes:
DGUOK  
(‡) Associated MGI genes:
Mpv17  

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* quick link - http://q.sanger.ac.uk/z4yfr6f2